Evidence map›Paper›PMID 23479743›Full record

ArticleThe Journal of cell biology2013

Rer1p maintains ciliary length and signaling by regulating γ-secretase activity and Foxj1a levels.

Nathalie Jurisch-Yaksi, Applonia J Rose, Huiqi Lu, Tim Raemaekers, Sebastian Munck, Pieter Baatsen, Veerle Baert, Wendy Vermeire, Suzie J Scales, Daphne Verleyen and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.3field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Cilia in the developing zebrafish ear.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2020
    Review
  4. Article
  5. RER1 enhances carcinogenesis and stemness of pancreatic cancer under hypoxic environment.Journal of experimental & clinical cancer research : CR · 2019
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Generation of multiciliated cells in functional airway epithelia from human induced pluripotent stem cells.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  15. Review
  16. Primary cilia and kidney injury: current research status and future perspectives.American journal of physiology. Renal physiology · 2013
    Review
  17. Article
  18. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors at 4 institutions in 2 countries.

Nathalie Jurisch-YaksiVIB Center for the Biology of Disease, KULeuven, 3000 Leuven, Belgium.
Applonia J Rose
Huiqi Lu
Tim Raemaekers
Sebastian Munck
Pieter Baatsen
Veerle Baert
Wendy Vermeire
Suzie J Scales
Daphne Verleyen
Roel Vandepoel
Przemko Tylzanowski
Emre Yaksi
Thomy de Ravel
H Joseph Yost
Guy Froyen
Cammon B Arrington
Wim Annaert
VIB-KU Leuven Center for Cancer Biology · BECenter for Human Genetics · USKU Leuven · BEUniversity of Utah · US

Funding

Establishing Left-Right Asymmetry in VertebratesK08HD062638 · NICHD · UNIVERSITY OF UTAH · PI ARRINGTON, CAMMON · 2010 to 2014
$686k
NICHD NIH HHS K08 HD062638NICHD NIH HHS K08HD062638
6 · The paper itself

Abstract

Cilia project from the surface of most vertebrate cells and are important for several physiological and developmental processes. Ciliary defects are linked to a variety of human diseases, named ciliopathies, underscoring the importance of understanding signaling pathways involved in cilia formation and maintenance. In this paper, we identified Rer1p as the first endoplasmic reticulum/cis-Golgi-localized membrane protein involved in ciliogenesis. Rer1p, a protein quality control receptor, was highly expressed in zebrafish ciliated organs and regulated ciliary structure and function. Both in zebrafish and mammalian cells, loss of Rer1p resulted in the shortening of cilium and impairment of its motile or sensory function, which was reflected by hearing, vision, and left-right asymmetry defects as well as decreased Hedgehog signaling. We further demonstrate that Rer1p depletion reduced ciliary length and function by increasing γ-secretase complex assembly and activity and, consequently, enhancing Notch signaling as well as reducing Foxj1a expression.

Indexed as

Adaptor Proteins, Vesicular TransportAmyloid Precursor Protein SecretasesAnimalsCell LineCiliaForkhead Transcription FactorsGene Expression RegulationHumansMembrane GlycoproteinsReceptors, NotchSignal TransductionSwineZebrafishZebrafish ProteinsAdaptor Proteins, Vesicular TransportAmyloid Precursor Protein SecretasesForkhead Transcription FactorsFoxj1a protein, zebrafishFOXJ1 protein, humanMembrane GlycoproteinsReceptors, NotchRER1 protein, humanZebrafish Proteins

Identifiers

PMID23479743
PMCPMC3601348
OpenAlexW2116457134

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.